Canonical Allele Identifier: CA1177626563

Gene: NEXN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.77943074_77943077delinsCCTA , CM000663.2:g.77943074_77943077delinsCCTA	GRCh38
NC_000001.10:g.78408759_78408762delinsCCTA , CM000663.1:g.78408759_78408762delinsCCTA	GRCh37
NC_000001.9:g.78181347_78181350delinsCCTA	NCBI36
NG_016625.1:g.59560_59563delinsCCTA , LRG_442:g.59560_59563delinsCCTA
NG_033243.2:g.41017_41020delinsTAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334785.12:c.*245_*248delinsCCTA MANE Select	ENSP00000333938.7:n.*245_*248delinsCCTA
ENST00000330010.12:c.*245_*248delinsCCTA	ENSP00000327363.8:n.*245_*248delinsCCTA
ENST00000334785.11:c.*245_*248delinsCCTA	ENSP00000333938.7:n.*245_*248delinsCCTA
ENST00000342754.5:c.1891_1894delinsCCTA
ENST00000480732.2:n.1847_1850delinsCCTA
NM_001172309.1:c.*245_*248delinsCCTA	NP_001165780.1:n.*245_*248delinsCCTA
NM_144573.3:c.*245_*248delinsCCTA , LRG_442t1:c.*245_*248delinsCCTA	NP_653174.3:n.*245_*248delinsCCTA
XM_005271322.2:c.*161_*164delinsCCTA	XP_005271379.1:n.*161_*164delinsCCTA
XM_005271323.2:c.*161_*164delinsCCTA	XP_005271380.1:n.*161_*164delinsCCTA
XM_005271324.3:c.*161_*164delinsCCTA	XP_005271381.1:n.*161_*164delinsCCTA
XM_005271325.2:c.*161_*164delinsCCTA	XP_005271382.1:n.*161_*164delinsCCTA
XM_005271326.2:c.*161_*164delinsCCTA	XP_005271383.1:n.*161_*164delinsCCTA
XM_005271327.2:c.*161_*164delinsCCTA	XP_005271384.1:n.*161_*164delinsCCTA
XM_005271322.4:c.*161_*164delinsCCTA	XP_005271379.1:n.*161_*164delinsCCTA
XM_005271323.4:c.*161_*164delinsCCTA	XP_005271380.1:n.*161_*164delinsCCTA
XM_005271324.5:c.*161_*164delinsCCTA	XP_005271381.1:n.*161_*164delinsCCTA
XM_005271325.4:c.*161_*164delinsCCTA	XP_005271382.1:n.*161_*164delinsCCTA
XM_005271326.4:c.*161_*164delinsCCTA	XP_005271383.1:n.*161_*164delinsCCTA
XM_005271327.4:c.*161_*164delinsCCTA	XP_005271384.1:n.*161_*164delinsCCTA
NM_001172309.2:c.*245_*248delinsCCTA	NP_001165780.1:n.*245_*248delinsCCTA
NM_144573.4:c.*245_*248delinsCCTA MANE Select	NP_653174.3:n.*245_*248delinsCCTA